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7th Annual International Meeting For Autism Research ... - Confex

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Program<br />

10:00 13 104.13<br />

Production Of Emotional Prosody And Facial Expressions In<br />

Adolescents With <strong>Autism</strong>. R. B. Grossman* 1 , L. R. Edelson 1 , L. B.<br />

Rubinstein 2 , J. Lomibao 3 , S. Borawski 1 and H. Tager-Flusberg 1 ,<br />

(1)Boston University School of Medicine, (2)Boston University,<br />

(3)Boston <strong>Autism</strong> Consortium<br />

10:00 14 104.14<br />

Do joint attention problems persist in verbal children with<br />

autism?. K. Leadbitter* and C. Lewis, Lancaster University<br />

11:00 15 104.15<br />

Acquisition of Social-Communicative Behavior in Toddlers at<br />

Risk for <strong>Autism</strong> Spectrum Disorders. W. J. Guthrie* 1 , C. Lord 1 ,<br />

M. Coffing 2 , R. Petrak 1 , R. Niehus 1 and S. Risi 1 , (1)University<br />

of Michigan <strong>Autism</strong> and Communication Disorders Center, (2)<br />

Vanderbilt University<br />

11:00 16 104.16<br />

Joint Attention in Infants and Toddlers with an <strong>Autism</strong><br />

Spectrum Disorder: <strong>Research</strong> into the Underlying Processes. I.<br />

Schietecatte* and H. Roeyers, Ghent University<br />

Poster Presentations<br />

105 Human Genetics Posters 1<br />

8:30 AM - 1:00 PM - Champagne Terrace/Bordeaux<br />

12:00 17 105.1<br />

The DLX1and DLX2 Genes and Susceptibility to <strong>Autism</strong><br />

Spectrum Disorders. X. Liu* 1 , N. Novosedlik 1 , M. Hudson 1 , A.<br />

Wang 1 , I. L. Cohen 2 , A. Chudley 3 , C. <strong>For</strong>ster-Gibson 1 , S. M. Lewis 4<br />

and J. J. Holden 1 , (1)Queen’s Univerity, (2)NYS Institute for<br />

Basic <strong>Research</strong> in Developmental Disabilities, (3)University of<br />

Manitoba, (4)University of British Columbia<br />

11:00 18 105.2<br />

Yield of Standard Genetic Testing in a Large <strong>Autism</strong> Diagnostic<br />

Clinic. P. Manning-Courtney* and J. Ruschman, University of<br />

Cincinnati<br />

12:00 19 105.3<br />

Biochemical And Genetic Studies Of The Mitochondrial<br />

Aspartate/Glutamate Carrier AGC1. L. Palmieri 1 , V. Papaleo 2 , V.<br />

Porcelli 1 , P. Scarcia 1 , R. Sacco 2 , J. Hager 3 , F. Rousseau 3 and A.<br />

M. Persico* 2 , (1)Univ. of Bari, (2)Univ. Campus Bio-Medico, (3)<br />

IntegraGen<br />

12:00 20 105.4<br />

Reelin Gene Expression And Epigenetic Status In Temporal<br />

Cortex Of Autistic Brains. C. Lintas* 1 , K. Garbett 2 , K. Mirnics 2 and<br />

A. M. Persico 1 , (1)Univ. Campus Bio-Medico, (2)Vanderbilt Univ.<br />

11:00 21 105.5<br />

A genome-wide association study of autism. X. Q. Liu* 1 , A. P.<br />

Thompson 2 , D. Pinto 1 , J. Skaug 1 , L. Zwaigenbaum 3 , W. Roberts 1 ,<br />

S. W. Scherer 1 , P. Szatmari 2 and A. D. Paterson 1 , (1)The Hospital<br />

for Sick Children, (2)Offord Centre for Child Studies, McMaster<br />

University, (3)Glenrose Rehab Hospital/ University of Alberta<br />

11:00 22 105.6<br />

Cognitive And Behavioral Characterization Of The Potocki-<br />

Lupski Syndrome. D. E. Treadwell-Deering* 1 , M. P. Powell 1 , J.<br />

R. Lupski 2 and L. Potocki 1 , (1)Texas Children’s Hospital, Baylor<br />

College of Medicine, (2)Baylor College of Medicine<br />

11:00 23 105.7<br />

Descriptive Analysis of 252 Twin Sets Recruited Through a<br />

National Online ASD Registry and <strong>Research</strong> Database. K. Law*,<br />

A. Marvin, C. Anderson, C. Cohen and P. Law, Kennedy Krieger<br />

Institute<br />

12:00 24 105.8<br />

Human Cerebellar Malformations and <strong>Autism</strong> Share<br />

Susceptibility Loci. K. A. Aldinger* 1 , I. D. Krantz 2 , W. B. Dobyns 1<br />

and K. J. Millen 1 , (1)The University of Chicago, (2)The Children’s<br />

Hospital of Phialdelphia<br />

11:00 25 105.9<br />

Replication and Association Analysis of a 1p13-q12 Locus<br />

for Nonverbal Communication Deficits in <strong>Autism</strong> Spectrum<br />

Disorder. J. L. Yoon, M. Alarcon, D. Geschwind and R. M.<br />

Cantor*, UCLA<br />

11:00 26 105.10<br />

Detecting Cognitive Endophenotypes for <strong>Autism</strong> Using a General<br />

Population Twin Family Sample. R. A. Hoekstra* 1 , M. Bartels 2 , G.<br />

F. Estourgie-van Burk 2 , S. Baron-Cohen 1 and D. I. Boomsma 2 , (1)<br />

University of Cambridge, (2)VU University<br />

11:00 27 105.11<br />

The relationship between molecular subtype and autism<br />

symptom severity in Angelman Syndrome. S. U. Peters* 1 , L. M.<br />

Bird 2 , R. Barbieri-Welge 2 , W. H. Tan 3 , R. Hundley 3 , S. Skinner 4 , A.<br />

Bauer-Carlin 4 , T. Sahoo 1 and C. A. Bacino 1 , (1)Baylor College of<br />

Medicine, (2)Rady Children’s Hospital San Diego, (3)Childrens<br />

Hospital Boston/Harvard Medical School, (4)Greenwood<br />

Genetics Center<br />

11:00 28 105.12<br />

Differences in Clinical Presentation of Trisomy 21 with and<br />

without <strong>Autism</strong>. C. A. Molloy* 1 , D. S. Murray 1 , H. Castillo 1 , F. J.<br />

Hickey 1 , B. Patterson 1 and A. Kinsman 2 , (1)Cincinnati Children’s<br />

Hospital Medical Center, (2)Greenville Hospital System<br />

Children’s Hospital<br />

12:00 29 105.13<br />

CADHERIN-11 as a possible candidate gene for autism. A.<br />

C. Crepel* 1 , H. Peeters 1 , J. R. Vermeesch 1 , J. Steyaert 2 , D.<br />

Walleghem 3 and K. Devriendt 1 , (1)University of Leuven, (2)<br />

University of Leuven, and Dept. Clinical Genetics, University of<br />

Maastricht, Netherlands, (3)University Center for Child and Youth<br />

Psychiatry<br />

12:00 30 105.14<br />

Association of MET with <strong>Autism</strong> Spectrum Disorder and Co-<br />

Occurring Gastrointestinal Symptoms. D. B. Campbell* 1 , T. M.<br />

Buie 2 , H. S. Winter 2 , M. Bauman 2 , J. S. Sutcliffe 1 , J. M. Perrin 2<br />

and P. Levitt 1 , (1)Vanderbilt University, (2)Massachusetts General<br />

Hospital for Children<br />

11:00 31 105.15<br />

Genomic Copy Number And Phenotypic Variability Of The<br />

<strong>Autism</strong> Spectrum Disorders. Y. Qiao* 1 , X. Liu 2 , M. Koochek 1 ,<br />

N. Riendeau 1 , P. Malenfant 2 , C. Harvard 1 , J. Hildebrand 1 , J. J.<br />

Holden 2 , E. Rajcan-Separovic 1 and S. M. Lewis 1 , (1)University of<br />

British Columbia, (2)Queen’s Univerity<br />

11:00 32 105.16<br />

Rate of Chromosomal Anomalies in an Iranian <strong>Autism</strong> Sample.<br />

A. Tolouei 1 , R. Sasanfar 2 , S. Haddad 3 , M. Houshmand 4 , M.<br />

Rostami 5 and S. L. Santangelo* 2 , (1)Special Education<br />

Organization of Iran, (2)Harvard Medical School, (3)Center for<br />

Human Genetic <strong>Research</strong>, (4)National Institute for Genetic<br />

Engineering and Biotechnology, (5)Medical Molecular Genetic<br />

Laboratory<br />

12:00 33 105.17<br />

Expression and methylation of the serotonin transporter gene<br />

in lymphoblastoïde cell lines from autistic patients carrying<br />

different genotypes for 5–HTTLPR. P. Vourc’h* 1 , R. Tabagh 1 , S.<br />

Védrine 1 , C. Barthelemy 2 , C. Moraine 1 and C. R. Andres 1 , (1)<br />

INSERM U930, University François-Rabelais de Tours, (2)CHRU<br />

de Tours, INSERM U930, University François-Rabelais of Tours<br />

14 7 th <strong>Annual</strong> <strong>International</strong> <strong>Meeting</strong> <strong>For</strong> <strong>Autism</strong> <strong>Research</strong> (IMFAR) 2008

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